Variant (rsID / SNP)
rs4987105
rs4987105 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALOX5. Location: chromosome 10, position 45,869,748. The table records no clinical significance for this variant.
Reference-table entries
ALOX5Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 10:45869748
- HGVS
- NM_000698.5,c.21C>T,p.Thr7Thr
- Allele change
- Silent
Associated conditions / phenotypes
Gestational Diabetes|Asthma|Atherosclerosis Susceptibility|Adult Respiratory Distress Syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.